258 related articles for article (PubMed ID: 11454185)
1. Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.
Campo S; Restuccia T; Villari D; Raffa G; Cucinotta D; Squadrito G; Pollicino T; Raimondo G
Liver; 2001 Aug; 21(4):233-6. PubMed ID: 11454185
[TBL] [Abstract][Full Text] [Related]
2. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
Trifa AP; Popp RA; Militaru MS; Farcaş MF; Crişan TO; Gana I; Cucuianu A; Pop IV
J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
[TBL] [Abstract][Full Text] [Related]
3. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
Cukjati M; Vaupotic T; Rupreht R; Curin-Serbec V
BMC Med Genet; 2007 Nov; 8():69. PubMed ID: 18036208
[TBL] [Abstract][Full Text] [Related]
4. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
Barton JC; Sawada-Hirai R; Rothenberg BE; Acton RT
Blood Cells Mol Dis; 1999; 25(3-4):147-55. PubMed ID: 10575540
[TBL] [Abstract][Full Text] [Related]
5. S65C and other mutations in the haemochromatosis gene in the Czech population.
Cimburová M; Půtová I; Provazníková H; Pintérová D; Horák J
Folia Biol (Praha); 2005; 51(6):172-6. PubMed ID: 16419611
[TBL] [Abstract][Full Text] [Related]
6. HFE gene mutations an Apulian population: allele frequencies.
Pietrapertosa A; Vitucci A; Campanale D; Palma A; Renni R; Delios G; Tannoia N
Eur J Epidemiol; 2003; 18(7):685-9. PubMed ID: 12952143
[TBL] [Abstract][Full Text] [Related]
7. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC
Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
[TBL] [Abstract][Full Text] [Related]
8. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
[TBL] [Abstract][Full Text] [Related]
9. Frequency of the HFE gene mutations in five Italian populations.
Candore G; Mantovani V; Balistreri CR; Lio D; Colonna-Romano G; Cerreta V; Carru C; Deiana L; Pes G; Menardi G; Perotti L; Miotti V; Bevilacqua E; Amoroso A; Caruso C
Blood Cells Mol Dis; 2002; 29(3):267-73. PubMed ID: 12547216
[TBL] [Abstract][Full Text] [Related]
10. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
de Diego C; Murga MJ; Martínez-Castro P
Genet Test; 2004; 8(3):263-7. PubMed ID: 15727249
[TBL] [Abstract][Full Text] [Related]
11. HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls.
de Juan D; Reta A; Castiella A; Pozueta J; Prada A; Cuadrado E
Eur J Hum Genet; 2001 Dec; 9(12):961-4. PubMed ID: 11840200
[TBL] [Abstract][Full Text] [Related]
12. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
Hellerbrand C; Bosserhoff AK; Seegers S; Lingner G; Wrede C; Lock G; Schölmerich J; Büttner R
Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
[TBL] [Abstract][Full Text] [Related]
13. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
Milić S; Ristić S; Starčević-Čizmarević N; Brajenović-Milić B; Crnić-Martinović M; Kapović M; Peterlin B; Štimac D
Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608
[TBL] [Abstract][Full Text] [Related]
14. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis.
Mura C; Raguenes O; Férec C
Blood; 1999 Apr; 93(8):2502-5. PubMed ID: 10194428
[TBL] [Abstract][Full Text] [Related]
15. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.
Cassanelli S; Pignatti E; Montosi G; Garuti C; Mariano M; Campioli D; Carbonieri A; Baldini E; Pietrangelo A
J Hepatol; 2001 Apr; 34(4):523-8. PubMed ID: 11394651
[TBL] [Abstract][Full Text] [Related]
16. HFE mutations, iron deficiency and overload in 10,500 blood donors.
Jackson HA; Carter K; Darke C; Guttridge MG; Ravine D; Hutton RD; Napier JA; Worwood M
Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
[TBL] [Abstract][Full Text] [Related]
18. Analysis of HFE-codon 63/282 (H63D/C282Y) gene variants in mexican mestizos. Blood donors and patients with hereditary hemochromatosis.
Ruiz-Argüelles GJ; Garcés-Eisele J; Gelbart T; Monroy-Barreto M; Reyes-Núñez V; Juárez-Morales JL; de Lourdes González-Garrido M; Ramírez-Cisneros FJ; Gallegos-Antúnez D
Arch Med Res; 2000; 31(4):422-4. PubMed ID: 11068087
[TBL] [Abstract][Full Text] [Related]
19. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
Milman N; á Steig T; Koefoed P; Pedersen P; Fenger K; Nielsen FC
Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317
[TBL] [Abstract][Full Text] [Related]
20. Genetic hemochromatosis, a Celtic disease: is it now time for population screening?
Byrnes V; Ryan E; Barrett S; Kenny P; Mayne P; Crowe J
Genet Test; 2001; 5(2):127-30. PubMed ID: 11551098
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
